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Senior Statistical Analyst - Programming - Oncology (Hybrid

Job in South San Francisco, San Mateo County, California, 94083, USA
Listing for: AbbVie
Full Time position
Listed on 2026-08-03
Job specializations:
  • IT/Tech
    Data Scientist, Data Analyst, Data Engineering
Salary/Wage Range or Industry Benchmark: 96500 - 183500 USD Yearly USD 96500.00 183500.00 YEAR
Job Description & How to Apply Below
Position: Senior Statistical Analyst - Programming - Oncology (Hybrid)

Senior Statistical Analyst
- Programming
- Oncology (Hybrid)

  • Full-time
  • Salary Min: 96500
  • Salary Max: 183500
  • Workday Global Grade: 17
  • Compensation: USD 96500 - USD 183500 - yearly

About Abb Vie

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us  .

Follow @abbvie onLinked

In, Facebook ,Instagram ,X and YouTube.

The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.

Responsibilities:

Leads the statistical programming activities for projects with lower complexity.

  • Leads the statistical programming activities for studies.
  • Develop SAS programs for the creation of ADaM data sets following CDISC standards.
  • Develop SAS programs for the creation of Tables, Listings and Figures.
  • Validation of ADaM data sets, Tables, Listings and Figures.
  • Create specifications for the structure of ADaM data sets for individual studies and integrated data.
  • Create documentation for regulatory filings including reviewers guides and data definition documents
  • Leads the development of standard SAS Macros and participates in the development of standard operating procedures.
  • Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.

Minimum Qualifications:

  • Bachelors in Statistics, Computer Science or a related field
  • 8+ years of relevant experience in quantitative analysis (or 6+ with a Masters)
  • Experience with SAS Programming
  • Experience leading programming for clinical trials

Preferred Qualifications:

  • Masters Degree in Statistics, Computer Science or related field
  • R Programming experience
  • Oncology specific experience

Other

Required Skills:

  • Indepth understanding of SAS programming concepts and techniques related to drug development.
  • Fundamental understanding of CDISC Standards.
  • Fundamental understanding of the drug development process, including experience with regulatory filings.
  • Ability to communicate clearly both oral and written.
  • Ability to accurately estimate effort required for study related programming activities.

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

  • The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.

    Individual compensation paid within this range will depend on many factors including geographic location,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible toparticipatein our short-term incentive programs.

Note:

No amount of payis considered to bewages or compensation until such amount is earned, vested, and determinable.

Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent with applicable law.

Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico applicants seeking a reasonable accommodation,  to learn more:

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Position Requirements
10+ Years work experience
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